A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385494



Internal ID21043047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70117501..70178400hg38UCSC Ensembl
chr4:70983218..71044117hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3860900
hg1960900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5325n223
Supporting Variantsnssv18211711
Samples
Known GenesC4orf40, CSN1S2BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385494
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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